Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Oxygen | HCID 977 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Dimethyl Sulfide | HCID 1068 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 131719814 | HCID 131719814 | — |
| Solvent | Dichloromethane methanol | HCID 21226129 | — |
| Product | HCID 88377828 | HCID 88377828 | — |
Reaction Steps
Combine (S)-N-benzyl-N-methyl-2-[N'-(t-butoxycarbonyl)-allylamino]-3-(naphth-2-yl)-propionamide (3.34 g, 7.29 mmol), and pyridine (0.03 ml) in dichloromethane/methanol (66 mL/7 mL). Cool to -78° C. Pass ozonized oxygen through the solution until a persistent light blue color is obtained. Pass nitrogen through the solution until the blue color dissipates. Add dimethyl sulfide (12 mL). Allow the reaction mixture to warm to ambient temperature and stir for 16 hours. Concentrate in vacuo to obtain a residue. Dilute the residue with ethyl acetate and extract with water. Separate the layers, dry the organic layer over MgSO4, filter, and evaporate in vacuo. Chromatograph on silica gel eluting with 20% ethyl acetate/hexane to give the title compound: TLC Rf =0.70 (silica gel, 50% ethyl acetate/hexane).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05597845 |
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| Source dataset | uspto-grants-1997_01 |
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| ORD ID | ord-fa4de417affc4ba9a38c002081838471 |
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| Source note | uspto-grants-1997_01 |
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